Canonical Allele Identifier: CA340729661

Gene: IL23R

Linked Data

• MyVariant Identifiers: chr1:g.67724717G>A (hg19) ; chr1:g.67259034G>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.67259034G>A , CM000663.2:g.67259034G>A	GRCh38
NC_000001.10:g.67724717G>A , CM000663.1:g.67724717G>A	GRCh37
NC_000001.9:g.67497305G>A	NCBI36
NG_011498.1:g.97549G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000697149.1:c.1635G>A	ENSP00000513138.1:n.1635G>A
ENST00000697150.1:c.1693G>A	ENSP00000513139.1:n.1693G>A
ENST00000697151.1:c.1626G>A	ENSP00000513140.1:n.1626G>A
ENST00000697164.1:c.1706G>A	ENSP00000513153.1:p.Gly569Glu
ENST00000697165.1:c.1493G>A	ENSP00000513154.1:p.Gly498Glu
ENST00000347310.10:c.1796G>A MANE Select	ENSP00000321345.5:p.Gly599Glu
ENST00000637002.1:c.1187G>A	ENSP00000490340.1:p.Gly396Glu
ENST00000347310.9:c.1796G>A	ENSP00000321345.5:p.Gly599Glu
ENST00000395227.2:c.590G>A	ENSP00000378652.2:p.Gly197Glu
ENST00000425614.3:c.1031G>A	ENSP00000387640.2:p.Gly344Glu
ENST00000473881.2:c.*622G>A	ENSP00000486667.1:n.*622G>A
NM_144701.2:c.1796G>A	NP_653302.2:p.Gly599Glu
XM_005270516.2:c.1034G>A	XP_005270573.1:p.Gly345Glu
XM_011540789.1:c.1886G>A	XP_011539091.1:p.Gly629Glu
XM_011540790.1:c.1796G>A	XP_011539092.1:p.Gly599Glu
XM_011540791.1:c.1796G>A	XP_011539093.1:p.Gly599Glu
XM_011540790.3:c.1796G>A	XP_011539092.1:p.Gly599Glu
XM_011540791.3:c.1796G>A	XP_011539093.1:p.Gly599Glu
XR_001736993.1:n.1876G>A
NM_144701.3:c.1796G>A MANE Select	NP_653302.2:p.Gly599Glu